Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome: Clinical and neuropathological observations in a 33-year-old man

American Journal of Medical Genetics

Volumn 78, Issue 4, 1998, Pages 371-377

  Keyvani, K ^a   Paulus, W ^a   Traupe, H ^b   Kiesewetter, F ^a   Cursiefen, C ^a   Huk, W ^a   Raab, K ^c   Orth, U ^d   Rauch, A ^a   Pfeiffer, R A ^a,e  

^a UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

^b UNIVERSITY OF MÜNSTER   (Germany)

^c Cnopfsche Kinderklinik   (Germany)

^d UNIVERSITY OF HAMBURG   (Germany)

^e UNIVERSITY HOSPITAL ERLANGEN   (Germany)

Author keywords

Alopecia; Ichthyosis follicularis; IFAP syndrome; Olivocerebellar atrophy; Photophobia

Indexed keywords

ADULT; ALOPECIA; ARTICLE; AUTOPSY; CASE REPORT; CONGENITAL ICHTHYOSIFORM ERYTHRODERMA; HUMAN; HUMAN TISSUE; MALE; MENTAL DEFICIENCY; MOTOR RETARDATION; MYOCLONUS SEIZURE; NEUROPATHOLOGY; OLIVOPONTOCEREBELLAR ATROPHY; PHOTOPHOBIA; PRIORITY JOURNAL; SYNDROME; TEMPORAL LOBE; X CHROMOSOME;

ABNORMALITIES, MULTIPLE; ALOPECIA; BLINDNESS; BRAIN; DIAGNOSIS, DIFFERENTIAL; FATAL OUTCOME; HUMANS; ICHTHYOSIS; ICHTHYOSIS, X-LINKED; INFANT, NEWBORN; LIGHT; MAGNETIC RESONANCE IMAGING; MALE; MENTAL RETARDATION; PSYCHOMOTOR DISORDERS; SEIZURES; SYNDROME; VISION DISORDERS;

EID: 0031880121     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19980724)78:4<371::AID-AJMG13>3.0.CO;2-F     Document Type: Article

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